Revealing how cytoskeletal dynamics form the early mammalian embryo
Revealing how cytoskeletal dynamics form the early mammalian embryo
批准号:
10624808
负责人:
Nicolas Daniel Plachta
金额:
$50.06万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-04-01 至 2026-03-31
关键词:
ActinsApicalAutomobile DrivingCell CommunicationCell Differentiation processCell LineageCell NucleusCell PolarityCell SeparationCell divisionCellsCytokeratin filamentsCytoplasmCytoskeletonDataDevelopmentElementsEmbryoEventF-ActinFetusFilamentFutureGoalsImageImplantInheritedInner Cell MassIntermediate FilamentsInterphaseKeratinLengthMammalian CellMeasurementMechanicsMicrotubulesMitosisModelingMolecularMolecular ChaperonesMovementMusNonmammalian EmbryoNuclearOrganismPARD6A genePatternPlacentaPregnancyProcessProteinsRoleSpecific qualifier valueTestingTimeUterusWorkbiophysical propertiesbiophysical techniquesblastocystblastomere structurecell cortexcell typedaughter cellembryo cellembryo stage 2genetic risk factorimaging approachin vivomechanical forcemolecular asymmetrymolecular dynamicsmouse developmentoverexpressionpreimplantationprematurescaffoldsegregationtranscription factor
中文摘要
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英文摘要
SUMMARY
Revealing the key events that specify the first differentiated cell lineages during mammalian development is key
to understand how the early embryo is organized to implant in the uterus and establish a pregnancy. The first
mammalian cell lineages comprise the pluripotent inner cell mass (ICM) that will form the fetus, and the outer
trophectoderm that will form the placenta. Yet, the mechanisms explaining how these lineages differentiate are
unclear. In many non-mammalian embryos, asymmetrically inherited cell-fate determinants specify lineage fate,
yet similar mechanisms are thought to be absent during early mammalian development.
We have established live-imaging approaches to study cell and molecular dynamics during early mouse
development. Recently, we identified a new role for intermediate filaments assembled by keratins in lineage
specification. Our studies reveal that keratin filaments are asymmetrically inherited precisely during the cell
divisions that physically segregate the future ICM and trophectoderm. Moreover, the inheritance of these
filaments by the outer daughter cells helps to specify their trophectoderm identity and promote their maturation.
Thus, our main hypothesis is that keratin filaments function as a new form of asymmetrically inherited factor
specifying the first trophectoderm cells during development. To test this, we will reveal the mechanisms by which
keratins become asymmetrically inherited (Aim 1) and can bias cell fate (Aim 2).
We will first test how interactions with proteins present at the apical cell cortex, and the dynamics of the filaments
inside the cell, control their asymmetric inheritance by outer cells during cell division. We will then determine how
keratins can regulate key aspects of cell mechanics and polarity to control the distribution of the key transcription
factors that specify trophectoderm fate.
In summary, in this proposal we will address a fundamental open question about the specification of the first
differentiated cell lineages during mammalian development, and unveil some of the first functions of keratin
intermediated filaments during early mammalian development, which unlike those of other cytoskeletal elements
like microtubules and actin, remain largely unknown.
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Revealing how cytoskeletal dynamics form the early mammalian embryo
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批准号:10378489
-
项目类别:
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资助金额:$49.11万
-
财政年份:2021
-
负责人:Nicolas Daniel Plachta
-
依托单位:
Revealing how cytoskeletal dynamics form the early mammalian embryo
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批准号:10117399
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项目类别:
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资助金额:$51.4万
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财政年份:2021
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负责人:Nicolas Daniel Plachta
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批准号:10470177
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项目类别:
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资助金额:$44.14万
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财政年份:2020
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负责人:Nicolas Daniel Plachta
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依托单位:
Revealing how the mitotic spindle controls asymmetric cell division in vivo
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批准号:10100123
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项目类别:
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资助金额:$44.03万
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财政年份:2020
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Revealing how the mitotic spindle controls asymmetric cell division in vivo
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项目类别:
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资助金额:$44.14万
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财政年份:2020
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负责人:Nicolas Daniel Plachta
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依托单位:
国内基金
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批准号:81801519
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项目类别:青年科学基金项目
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批准年份:2018
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负责人:于岚
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依托单位: